Canonical Allele Identifier: CA382649058
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1950761643

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410789T>C , CM000673.2:g.113410789T>C GRCh38
NC_000011.9:g.113281511T>C , CM000673.1:g.113281511T>C GRCh37
NC_000011.8:g.112786721T>C NCBI36
NG_008841.1:g.69491A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1270A>G MANE Select ENSP00000354859.3:p.Ile424Val
ENST00000346454.7:c.1183A>G ENSP00000278597.5:p.Ile395Val
ENST00000362072.7:c.1270A>G ENSP00000354859.3:p.Ile424Val
ENST00000538967.5:c.1276A>G ENSP00000438215.1:p.Ile426Val
ENST00000542968.5:c.1270A>G ENSP00000442172.1:p.Ile424Val
ENST00000544518.5:c.1267A>G ENSP00000441068.1:p.Ile423Val
NM_000795.3:c.1270A>G NP_000786.1:p.Ile424Val
NM_016574.3:c.1183A>G NP_057658.2:p.Ile395Val
XM_017017296.2:c.1270A>G XP_016872785.1:p.Ile424Val
NM_000795.4:c.1270A>G MANE Select NP_000786.1:p.Ile424Val
NM_016574.4:c.1183A>G NP_057658.2:p.Ile395Val